Linked Data
gnomAD v4:
3-8745920-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8745920T>C , CM000665.2:g.8745920T>C | GRCh38 |
| NC_000003.11:g.8787606T>C , CM000665.1:g.8787606T>C | GRCh37 |
| NC_000003.10:g.8762606T>C | NCBI36 |
| NG_008797.2:g.17111T>C , LRG_329:g.17111T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343849.3:c.*53T>C MANE Select | ENSP00000341940.2:n.*53T>C | |
| ENST00000343849.2:c.*53T>C | ENSP00000341940.2:n.*53T>C | |
| ENST00000397368.2:c.*6+47T>C | ENSP00000380525.2:n.*6+47T>C | |
| ENST00000472766.1:n.155+11930T>C | ||
| NM_001234.4:c.*6+47T>C | NP_001225.1:n.*6+47T>C | |
| NM_033337.2:c.*53T>C , LRG_329t1:c.*53T>C | NP_203123.1:n.*53T>C | |
| NM_001234.5:c.*6+47T>C | NP_001225.1:n.*6+47T>C | |
| NM_033337.3:c.*53T>C MANE Select | NP_203123.1:n.*53T>C |